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Text-fig. 12. Paramblypterus cf. rohani. Arrows indicate directio cranialis. a, b: photograph and drawing of four ridge scales in front of the dorsal fin base, locality Otovice "Chmelnice", P 80178, scale bars 5 mm; c: scale rows from the area between the pectoral and pelvic fins, outer surfaces of the scales bear fine ridges terminating as denticles on the posterior edge of the scales, locality Otovice "Chmelnice", NM-M 4916, scale bar 5 mm; d: isolated scale, from anterior area of the lateral side of the body, with denticulated posterior edge, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; e: isolated scale from the pelvic area of the body, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; f, g: drawing and photograph of the postcleithrum and the scales behind the pectoral girdle (the scales bear conspicuous ridges on their outer surface; well preserved large postcleithrum is without ridges.), locality Otovice "Chmelnice", NM-M 4915, scale bars 5 mm. Abbreviations: Cl – cleithrum, Pcl – postcleithrum, Scl – supracleithrum. in Actinopterygians Of The Broumov Formation (Permian) In The Czech Part Of The Intra-Sudetic Basin (The Czech Republic)
Text-fig. 12. Paramblypterus cf. rohani. Arrows indicate directio cranialis. a, b: photograph and drawing of four ridge scales in front of the dorsal fin base, locality Otovice "Chmelnice", P 80178, scale bars 5 mm; c: scale rows from the area between the pectoral and pelvic fins, outer surfaces of the scales bear fine ridges terminating as denticles on the posterior edge of the scales, locality Otovice "Chmelnice", NM-M 4916, scale bar 5 mm; d: isolated scale, from anterior area of the lateral side of the body, with denticulated posterior edge, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; e: isolated scale from the pelvic area of the body, locality Otovice "Chmelnice", P 30945, scale bar 2 mm; f, g: drawing and photograph of the postcleithrum and the scales behind the pectoral girdle (the scales bear conspicuous ridges on their outer surface; well preserved large postcleithrum is without ridges.), locality Otovice "Chmelnice", NM-M 4915, scale bars 5 mm. Abbreviations: Cl – cleithrum, Pcl – postcleithrum, Scl – supracleithrum.
Text-fig. 3. CT slices on Block 3. Invertebrate moulds (a, c) and remains of their hard skeletons (a, b). Large areas of limestone matrix hold either only a few scattered invertebrates or no fossil at all (b, c). Ring artefacts seen close to the isocentre of the scan (b, c) are a well-known phenomenon caused by the X-ray beams traversing the block at an insufficient radiation dose (as expected in such a large block of dense material), and are not part of any physical structure present therein (Triche et al. 2019). in Hidden Treasures Uncovered: Successful Detection Of Fossils Below The Surface In Large Limestone Blocks Using A Standard Medical X-Ray Ct Scanner
Text-fig. 3. CT slices on Block 3. Invertebrate moulds (a, c) and remains of their hard skeletons (a, b). Large areas of limestone matrix hold either only a few scattered invertebrates or no fossil at all (b, c). Ring artefacts seen close to the isocentre of the scan (b, c) are a well-known phenomenon caused by the X-ray beams traversing the block at an insufficient radiation dose (as expected in such a large block of dense material), and are not part of any physical structure present therein (Triche et al. 2019).
Text-fig. 10. Langtonia bisulcata REID et CHANDLER. a, b, e–g: Holotype, V. 22984, from micro-CT data. a: Dorsiventral view surface rendering. b: Dorsiventral view translucent volume rendering showing outline of locule cast. c: Equatorial transverse fracture showing paired dorsal infolds and locules with shape of a ε in cross section, reflected light, V. 22993. d: Digital transverse section from micro-CT data, of fruit with two well developed ε-shaped locules, V. 22985. e–g: Successive digital transverse sections with one well developed ε-shaped locule and infolds of the abortive locule visible in (g) (arrows). h–j: Physical transverse thin sections of specimen from middle Eocene Clarno Formation, Oregon, USA with well-preserved mesocarp including longitudinal canals in (j) (arrows), USNM 424875; Scale bars 0.5 cm in (a, b), 2.5 mm in (c–g), 5 mm in (h), 2 mm in (i), 1 mm in (j); (a, b) share same scale bar; (c, d) share same scale bar; (e, f, g) share same scale bar. in Mastixioid Fruits (Cornales) From The Early Eocene London Clay Flora: Morphology, Anatomy And Nomenclatural Revision
Text-fig. 10. Langtonia bisulcata REID et CHANDLER. a, b, e–g: Holotype, V. 22984, from micro-CT data. a: Dorsiventral view surface rendering. b: Dorsiventral view translucent volume rendering showing outline of locule cast. c: Equatorial transverse fracture showing paired dorsal infolds and locules with shape of a ε in cross section, reflected light, V. 22993. d: Digital transverse section from micro-CT data, of fruit with two well developed ε-shaped locules, V. 22985. e–g: Successive digital transverse sections with one well developed ε-shaped locule and infolds of the abortive locule visible in (g) (arrows). h–j: Physical transverse thin sections of specimen from middle Eocene Clarno Formation, Oregon, USA with well-preserved mesocarp including longitudinal canals in (j) (arrows), USNM 424875; Scale bars 0.5 cm in (a, b), 2.5 mm in (c–g), 5 mm in (h), 2 mm in (i), 1 mm in (j); (a, b) share same scale bar; (c, d) share same scale bar; (e, f, g) share same scale bar.
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021). in Floristic, Vegetation And Climate Assessment Of The Early/Middle Miocene Parschlug Flora Indicates A Distinctly Seasonal Climate
Text-fig. 1. Modern vegetation proxies as delivered by the Drudge 1 and 2 tools for Parschlug. Left column results from KovarEder et al. (2021) based on the floristic spectrum published by Kovar-Eder et al. (2004). The other three columns result from three variants using the enlarged floristic spectrum herein. Differences between variants 1–3 from this study are caused by differences in assignment of some taxa and morphotypes (see Appendix 1). European vegetation formations: Formation C – Subarctic, boreal and nemoral-montane open woodlands as well as subalpine and oro-Mediterranean vegetation; Formation D – Mesophytic and hygromesophytic coniferous and mixed broad-leaved-coniferous forests; Formation F – Mesophytic broadleaved deciduous and mixed broadleaved/conifer forests; Formation G – Thermophilous mixed deciduous broadleaved forests; Formation J – Mediterranean sclerophyllous forests and scrub; Formation K – Xerophytic coniferous forests, coniferous woodland and scrub. East Asian vegetation types: MCF China, Japan – Montane Coniferous Forests China, Honshu, Yakushima; BLDF N and NE Provinces, China – Broad-leaved Deciduous Forests of the Northern and Northeastern Provinces (China); BLDF Upper Yangtze, Honshu – Broad-leaved Deciduous Forest, Upper Yangtze Provinces, Mt. Emei, and Honshu; MMF China – Mixed Mesophytic Forest, Lower Yangtze Provinces; BLEF China, Japan – Broad-leaved Evergreen Forests, China, Japan; Meili Snow Mt. high altitude SCL and BLF, China – Meili Snow Mt., Sclerophyllous and broad-leaved forest zone (2,580-3,650 m alt.). (Designations of European vegetation formations follow Bohn et al. (2004) and Asian ones follow Kovar-Eder et al. (2021).
Data from: Bratzel et al. (2022) Target-enrichment sequencing reveals for the first time a well-resolved phylogeny of the core Bromelioideae (Bromeliaceae). Taxon
<p>DNA sequence alignments used for phylogenetic analyses in Bratzel et al. (2022) Target-enrichment sequencing reveals for the first time a well-resolved phylogeny of the core Bromelioideae (Bromeliaceae). Taxon.</p>
Supplementary material 1 from: Gruber B, Evans D, Henle K, Bauch B, Schmeller D, Dziock F, Henry P, Lengyel S, Margules C, Dormann C (2012) "Mind the gap!" – How well does Natura 2000 cover species of European interest? Nature Conservation 3: 45-62. https://doi.org/10.3897/natureconservation.3.3732
The table shows the 54 gap species ordered by species group. Please note: The comment column is based on expert opinion of the European Topic Centre, which has the latest version of the Natura2000 data base and also knowledge on confidential sites, which are deleted from the public version of the data base to protect rare species.
BRAIN Journal-Brain-Like Artificial Intelligence for Automation-Figure 1. Examples for Today Well Manageable and not yet Well Manageable Processes in Automation
<p>Despite the many progresses that have been achieved in automation and AI over the last decades, applications have mainly been successful for circumscribed, well-defined tasks in environments that are relatively specific, well-structured, and characterized by a limited number of possible occurring processes, states, and ways how to react to them [59]. There, technical solutions can even exceed certain human capabilities. The situation changes however if we switch to systems that should perform a broader range of tasks in less well-structured environments. Here, the limits of technical feasibility are being stretched to the utmost [7]. This fact is probably best illustrated by<br> the following two concrete examples in Figure 1.</p>
parallel-fibered bone; A5, osteocyte lacunae with well-preserved canaliculi; B3, osteocyte lacunae lacking canaliculi; B4, B5, growth pattern with preserved residuals of the thick annuli and zones (zo I–III) and thin annuli and zones (zo IV–VII); A6, growth pattern with preserved thin annuli and thick zones (zo I–IV), the dotted line marks the border between the perimedullary region and the cortex. Arrows in A5 and B3 indicate osteocyte lacunae; in B4, B5, and A6 indicate the annuli. Growth pattern in B4 figured on the lateral section side, in B5 and A5 on the ventral side; note the cortex thickness variation between B4 and B5. A1, A3, A4, A6, B1, B4, B5 in polarized light and A2, A5, B2, B3 in normal transmitted light. Abbreviations: an, annulus; ec, erosion cavity; pmr, perimedullary region; pos, primary osteon; sos, secondary osteon; zo, zone. in Palaeohistology helps reveal taxonomic variability in exceptionally large temnospondyl humeri from the Upper Triassic of Krasiejów, SW Poland
parallel-fibered bone; A5, osteocyte lacunae with well-preserved canaliculi; B3, osteocyte lacunae lacking canaliculi; B4, B5, growth pattern with preserved residuals of the thick annuli and zones (zo I–III) and thin annuli and zones (zo IV–VII); A6, growth pattern with preserved thin annuli and thick zones (zo I–IV), the dotted line marks the border between the perimedullary region and the cortex. Arrows in A5 and B3 indicate osteocyte lacunae; in B4, B5, and A6 indicate the annuli. Growth pattern in B4 figured on the lateral section side, in B5 and A5 on the ventral side; note the cortex thickness variation between B4 and B5. A1, A3, A4, A6, B1, B4, B5 in polarized light and A2, A5, B2, B3 in normal transmitted light. Abbreviations: an, annulus; ec, erosion cavity; pmr, perimedullary region; pos, primary osteon; sos, secondary osteon; zo, zone.
Replication Archive for "Teen Social Interactions and Well-being during the COVID-19 Pandemic"
<p><span>This archive includes the Stata code to replicate all results in the referenced paper.</span></p>
Spatial analysis of the potential impact of contaminated areas on wells and aquifers in the Upper Tietê Basin, São Paulo, Brazil
<p><span>Upper Tietê stands out as the basin with the highest concentration of contaminated areas in São Paulo, Brazil, thereby exerting a pronounced impact on the quality of groundwater and directly affecting the resident population. Recognizing the importance of developing indicators for effective aquifer management, this study proposed to identify and assess the degree of risk, vulnerability, and contamination of aquifers and wells in the Upper Tietê Basin. Were applied the Aquifer Vulnerability Index method to evaluate the aquifer vulnerability in the region; the delimitation of safety perimeters and identification of wells at risk; and the integrated risk index, unifying information on social and aquifer vulnerabilities, hazards and exposure. The results reveal that the aquifers have a high vulnerability, mainly due to the thickness of their unsaturated layer. Furthermore, there were 7,958 wells at risk around the basin (77.15%), and the most vulnerable municipalities are on the outskirts of the basin. This study provides important insights, mainly due to the holistic approach, serving as a basis for identifying the regions with the highest risks, which can be prevented and mitigated with appropriate actions.</span></p>
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats. in External and internal microbiomes of Antarctic nematodes are distinct, but more similar to each other than the surrounding environment
SI Figure 2: Compositional differences among bacterial microinvertebrate external and internal microbiomes as well as mats they were isolated from using Bray Curtis distance matrix visualized with a NMDS ordination. Circles indicate each community and stars show centroids of microbiome types for each animal host. All host microbiomes (internal and external) are distinct from mat communities (P<0.05), but external microbiomes are more similar to mats than internal microbiomes are to mats.
Dataset: Petco Health and Wellness Company, Inc. (WOOF) Stock Performance
This dataset provides historical stock market performance data for specific companies. It enables users to analyze and understand the past trends and fluctuations in stock prices over time. This information can be utilized for various purposes such as investment analysis, financial research, and market trend forecasting.
FIGURE 1. The 25 in Twenty-five well-justified fossil calibrations for primate divergences
FIGURE 1. The 25 fossil calibrations shown in phylogenetic context. 1 = Crown Euarchontoglires (Euarchonta-Glires split), 2 = Crown Glires (Rodentia-Lagomorpha split), 3 = Crown Euarchonta (Primatomorpha-Scandentia split), 4 = Crown Primatomorpha (Primates-Dermoptera split), 5 = Crown Primates (Haplorhini-Strepsirhini split), 6 = Crown Strepsirrhini (Lorisiformes-[Lemuriformes+Chiromyiformes] split), 7 = Lemuriformes+Chiromyiformes (Lemuriformes- Chiromyiformes split), 8 = Crown Lorisiformes (Lorisidae-Galagidae split), 9 = Crown Lorisidae (Lorisinae-Perodicticinae split), 10 = Crown Haplorhini (Anthropoidea-Tarsiiformes split), 11 = Crown Anthropoidea (Catarrhini-Platyrrhini split), 12 = Crown Catarrhini (Cercopithecoidea-Hominoidea split), 13 = Crown Cercopithecidae (Cercopithecinae- Colobinae split), 14 = Crown Colobinae (Colobini-Presbytini split), 15 = Crown Cercopithecinae (Cercopithecini-Papionini split), 16 = Crown Papionini (Macacina-Papionina split), 17 = Crown Cercopithecini(uncertain split), 18 = Crown Hominoidea (Hominidae-Hylobatidae split), 19 = Crown Hominidae (Homininae-Ponginae split), 20 = Homo+Pan (Homo-Pan split), 21 = Crown Platyrrhini (Pitheciidae-[Aotidae+Atelidae+Callitrichidae+Cebidae] split), 22 = Crown Pitheciidae (Callicebinae-Pitheciinae split), 23 = Callitrichidae+Cebidae (Callitrichidae-Cebidae split), 24 = Crown Cebidae (Cebinae-Saimirinae split), 25 = Crown Atelidae (Alouattinae-Atelinae split).
FIGURE 7 in A new species of Cricosaurus (Thalattosuchia, Metriorhynchidae) based upon a remarkably well-preserved skeleton from the Upper Jurassic of Germany
FIGURE 7. Cricosaurus albersdoerferi sp. nov. (BMMS-BK 1-2) holotype, late Kimmeridgian of Painten (Southern Germany). Limbs and girdle elements. (A) front limbs and pectoral girdle, (B) hind limbs and pelvis. Abbreviations: ast, astragalus; cal, calcaneum; co, coracoid; dt, distal tarsal; fe, femur; fi, fibula; h, humerus; il, ilium; mc, metacarpal; mt, metatarsal; ph, phalanx; pub, pubis; r, radius; re, radiale; sc, scapula; ti, tibia; u, ulna. Scale bars equal 50 mm.
FIGURE 6 in A new species of Cricosaurus (Thalattosuchia, Metriorhynchidae) based upon a remarkably well-preserved skeleton from the Upper Jurassic of Germany
FIGURE 6. Cricosaurus albersdoerferi sp. nov. (BMMS-BK 1-2) holotype, late Kimmeridgian of Painten (Southern Germany). Caudal vertebrae in lateral view. (A) proximal caudals, (B) distal caudal series and tail bend. Abbreviations: ap, anterior process; ffc, first flexural caudal vertebra; hp, hemapophysis; hs, hemapophyseal lobe; ns, neural spine. Scale bars equal 50 mm.
FIGURE 4 in A new species of Cricosaurus (Thalattosuchia, Metriorhynchidae) based upon a remarkably well-preserved skeleton from the Upper Jurassic of Germany
FIGURE 4. Cricosaurus albersdoerferi sp. nov. (BMMSBK 1-2) holotype, late Kimmeridgian of Painten (Southern Germany). Close-ups of the dentition (A) and scleral ring (B). Scale bars equal 10 mm.
FIGURE 3 in A new species of Cricosaurus (Thalattosuchia, Metriorhynchidae) based upon a remarkably well-preserved skeleton from the Upper Jurassic of Germany
FIGURE 3. Cricosaurus albersdoerferi sp. nov. (BMMS-BK 1-2) holotype, late Kimmeridgian of Painten (Southern Germany). Skull in lateral view with illustration of the preserved elements. Abbreviations: an, angular; art, articular; cor, coronoid; d, dentary; en, external naris; fr, frontal; hy, hyoid; jug, jugal; lac, lacrimal; mx, maxilla; ns, nasal; pmx, premaxilla; po, postorbital; pof, preorbital fenestra; prf, prefrontal;?qu, possible quadrate; sa, surangular; sdg, surangulodentary groove; sp, splenial;?sq, squamosal or squamosal-postorbital fragment. Scale bar equals 50 mm.
FIGURE 1 in A new species of Cricosaurus (Thalattosuchia, Metriorhynchidae) based upon a remarkably well-preserved skeleton from the Upper Jurassic of Germany
FIGURE 1. Cricosaurus albersdoerferi sp. nov. (BMMS-BK 1-2) holotype, late Kimmeridgian of Painten (Southern Germany). Skeleton in lateral view. Scale bar equals 200 mm.
The data on the optical properties of kombucha and kombucha proteinoids, as well as chaos calculations are provided for the paper titled "Kombucha Mats as Responsive Materials."
<p>The data on the optical properties of kombucha and kombucha proteinoids, as well as chaos calculations are provided for the paper titled "Kombucha Mats as Responsive Materials."</p>
species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola. in Diversity and Distribution of the Amphibians and Terrestrial Reptiles of Angola Atlas of Historical and Bibliographic Records (1840-2017)
species according to Broadley (1994). These may well be the result of continuing confusion over the placement of Keta. Given the localities known from Lunda Norte, it seems likely that the species occurs in other northern regions of Angola. MAP 363. Distribution of Scaphiophis albopunctatus in Angola.
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.